Stem Cell Treatment

more than 60 diseases can be treated with stem cells Read More...

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Multiple sclerosis treatment

Patient from Portugal, Diagnosed Multiple Sclerosis, One month after treatment he could walk again Read More...

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Swiss medica clinica

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NEW modern technology - activating autologous own stem cells and replacing the damaged cells

Patients satisfied with the stem cells therapy

  • Dear Jana and all at Belgrade clinic.

    I hope you are all well. Things are great here - my sleep is a lot better 6 hour stretches now and able to get back to sleep when disturbed, all without drugs for first time in 27 years. My legs are getting stronger thanks to the wonderful Physio and exercises. I can see a day in the near future when I won’t need a stick. My digestion is a lot better so no unconfortable tummy aches. I am a lot calmer and thinking clearer, the stress of illness has gone from my face which a lot of people have noticed, saying I look so well. I, will keep reporting, I am so happy (I thought I would never be well again but I am. Thanks to all of you).
    Have a great Christmas all at Belgrade. Love
  • Would you please pass on the following messages to my dear friends at the Moscow clinic.

    Please say hello to Katya and Liluba, who looked after me with such love and care, I will never forget their kindness. Hello to Tanya (no pain, normal). A special thanks to Alexandria with much love and best wishes for her future. I regret I didn't have the chance to say goodbye and thank you to Vitaliy Nikitin for all he did for me. Could you thank him from the bottom of my heart for his kindness and caring.

    There were just too many others to list individually here, but I would like to send a big thank you to all the staff who showed such love and kindness to myself and Denyse during our stay. Our stay at the clinic felt like being part of a large and loving family and I will cherish that memory forever.
  • Dear doctor,
    Uroš is staying healthy and happy and there are some changes in his condition. He is using a real toilet now; he do more things by himself - like taking clothes and shoes on and off, he is more interested in using pencil and crayons and he is playing with more toys than earlier.He did`t start talking yet, but he is often mumbling something. We finished giving him RNA medicines in January. We started giving him Chlorella 1000 mg 3 times a day on 12th of January and he is taking it well. Three days ago we did a check on Vitamin D3 and Calcium, so we are sanding you results. I hope you will respond and tell me your opinion about those results.
    Kindest regards,
    Stoja Senka
  • We think about you all the time and we often talk how nice it was staying in Clinic.

    We had realy nice time there. We told to all our friends about Clinic and people there. He feels more stabile on his legs and I can see a bit improvment in his walking.

    At the moment he is refusing to use roller walkek, he is walking with someone holding his hand. About his nervus it is a bit better. He is rune out of pils that we brought with us.
  • The driver came and pick us up, we went to clinic and I was shocked with the welcoming we received from the clinic. The staff was brilliant, my son was so much loved, and he felt really good.

    Since we had stem cell treatment it's been nine months. It's unbelievable how our life has changed. Mom is calmer, dad is calmer. Why? Because our son is happy, now.
  • I started to feel an improvement in my right leg. I can now lift my leg higher than I could before and I’m finding that walking up and down the stairs, I can walk without actually holding on to the banister. The level of service here has been absolutely second to none with all of the staff.

    The doctors are absolutely fantastic. The nurses, and the whole team…
  • There's familial atmosphere, rhythm, same people, kind words, and the medical staff is always available when you have a question, they come every day to see you.

    It is important, they do not come just because of the treatment, the doctors are everyday here to ask you how your day was, how you feel, if the treatment eas difficult or easy. There is no clinical atmosphere, no hospital smell. In hospitals there is always the smell of drugs. Here I don’t feel it at all. thisw is actually like a villa.
  • What else can I say? I am very very happy with all the care that I received and I recommend this treatment to anybody who want to give it a go. Come and have an open mind and meet these wonderful people who will treat you gently and with respect. I’ll always be grateful.

    Thank you.
  • Well, the first month went well. I regained my psychophysical energy, especially in the sport I practice, I felt an improvement...

    Now I hope, I hope that in the future, and the doctors tell me that it is better, I hope that in the future I'll feel all the better.
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Positive stories from ex MS patients after Stem Cell treatment

Client: Carla and Shaun

Country: UK

Shaun: Hi, my name is Shaun Lawrence and today I’ve come to my friend Carla’s house and together we would like to talk to you about our experiences, having stem cell treatment with Swiss Medica, to help us with our multiple sclerosis diagnosis.

Carla: My name is Carla Wallace-Clark. Like Shaun, I’m a MS sufferer. If you might hear Oscar in the background, our new puppy, which we’ve had since January, after my stem cell therapy treatment. Back in December, we couldn’t even entertain the fact of having a puppy and now we’re enjoying him.

Shaun: When I found myself looking for a clinic that could offer me this treatment with the stem cells, I soon found that there was absolutely nowhere in the UK, there was nothing that would help me. So I found myself looking abroad. There are many countries offering stem cells, with varying prices and slightly different procedures. The one that I opted for was Swiss Medica. I’ve always thought of Switzerland as being very much ahead of the times with medical practices and I felt very comfortable and decided that that was going to be for me.

Carla: Well I was diagnosed back in 2015. Diagnosed in the April and very quickly I went downhill. I was diagnosed with Relapse-Remitting MS. Diagnosed in the April, by the August I was bedridden. By the time we returned from our holiday, I was literally confined to my bed. I couldn’t do anything. I couldn’t take my children to school, I couldn’t do any of the extracurricular activities with them, I couldn’t cook for them, I couldn’t look after them, I couldn’t do any house work. I couldn’t do anything. I was good for nothing. The MS nurses and my neurologist said that I wasn’t ill enough to be prescribed disease-modifying drugs and I just had to look after myself. We found this very hard to live with, because MS has marred every aspect of my life. From my underwear, from the clothes that I wear, from the shoes that I had to wear, from the activities that I did, to the food that I ate, it marred absolutely every aspect of my life. So, it was causing a lot of distress. In the April a documentary came on the TV about stem cell therapy and it was the only thing that gave us spark, that gave it light at the end of the tunnel and I thought we can do this. Through family members we got to hear about Shaun and Shaun’s experience and after seeing that documentary, we set up a meeting for me to meet Shaun. And from then on it was almost plain sailing, without the nervousness and going into the unknown. But it was always a light at the end of the tunnel.

Shaun: So having decided to go with Swiss Medica I then was advised by the consultants to go to their Moscow clinic, who are specialists in neurological diseases.

Carla: So once we met Shaun and learned of his experiences we realized that stem cell therapy was the only way forward for us.

Shaun: So Carla, who would have believed to only 12 months ago, we would have been sitting here today and talking about the things that we have. Isn’t it just amazing?

Carla: Shaun, it incredible! I’ll be forever indebted to you, actually, because if it wasn’t for your encouragement, I don’t know where we’d be. I really don’t know where we’d be. It’s just been amazing, a dream come true. A real dream come true.

Shaun: I think it’s important for each of us to support each other and for other people that have got similar diseases, I think it’s important to have that support, isn’t it?

Carla: Oh, absolutely. And also to talk as well. It’s important to talk. Sometimes talking is a therapy in itself, but it also reminds you of what was, what has been and what can be. And I am so excited.

Shaun: And also, that you’re not alone in how you feel. I think sometimes you think that it’s only ever happening to you, but actually, it is relevant to a lot of people.

Carla: It really is and you know, I used to think that it is in my head and so then I’d try and do things and then that would have fallen over. Because it wasn’t in my head, this was actually really happening. You know, incident is tripping over a piece of string, you know, not making it to the loo in time, not being able to get out of bed and just getting up and collapsing on the floor. Just all these silly things that happen and it’s not just you, the amount of people that are suffering and suffering unnecessarily, because there is something out there.

Shaun: There is.

Carla: You know, there is. And I still don’t understand why they didn’t think that I could have disease-modifying drugs, but you know, they did me a favor, because this is so much better. I don’t know how long it will last for, we don’t know, but at the moment it is fantastic, I’m enjoying every day.

Shaun: I think, as you will probably agree with me, to have a positive attitude is the way forward. When you have an off day, you have to rise above it and you have to look to tomorrow and say “Tomorrow, I’m gonna make this better.”

Carla: Oh yeah, absolutely.

Shaun: And you’re the same. I’m sure we’re both very positive people and that’s why we’re here Carla.

Carla: Or just plain stubborn.

Shaun: So Carla, how are things with you now?

Carla: Absolutely brilliant. Absolutely brilliant! I can do things that back in December I couldn’t imagine. I mean, we’re talking 2 months ago! I couldn’t imagine. I’m walking Toby to school, we’ve got the new puppy, so I’m doing circuits in the garden. I have seen more of my garden in this past month than I had in 2 years! I’ve seen bits that I’ve just not been able to get to, because I couldn’t make it. I’ve been able to walk up and down the drive. It’s been incredible. We couldn’t have entertained a puppy back in December and now I’m looking after a puppy, which is like looking after a newborn child. I’m swimming twice a week on top of that, up to 22 lengths twice a week. December I was at 0, so that is fantastic, to me that’s my achievement. In the next month I’m planning to include yoga on top of that and also I’m gonna be doing a walk for charity 10.000 steps a day for cancer research. So that’s me doing that, that’s me being stubborn and not letting this MS get to me. I’m also looking forward to doing family walks at Bickerton Hill and pub lunches again, because it’s not a problem, whether I’d make it around or whether I’d need a toilette stop halfway up the hill. You know, it’s just incredible. And then we’ve booked a family holiday, because we can, we didn’t go on one last year, because I just wasn’t any good, but this year we’re going sailing. So the last time we went sailing, I was below deck because I was wiped out, MS has knocked me for six. This time I’m gonna be sailing that boat. I’m so excited! Life is exciting. Every day is a new day and I am just so appreciative. Shaun, thank you again for giving me that kick up the backside to book that ticket and go.

Shaun: You’ve done it yourself.

Carla: Thank you. What have you got planned for this year?

Shaun: I’m hoping to go on holiday and just enjoy life. Just enjoy life. What about you?

Carla: Well, as I’ve said, we’ve got the new puppy, so daily walks. I’ve started swimming, next month I plan to do yoga.

Shaun: Yoga?! Wow!

Carla: Yes! I’m gonna do a charity walk, 10.000 steps a day for cancer research, I’m planning on doing that.

Shaun: Well done.

Carla: I’m looking forward to going on a family walk up the Bickerton Hill, which is close by. We’ve booked a family holiday, we’re going sailing.

Shaun: Wow!

Carla: Because the last time we went sailing I was below deck, because I was just whipped out, but this time I’m gonna be sailing that boat.

Shaun: You’re gonna be operating that boat!

Carla: Yes! So I’m really excited, I’m enjoying each day. And yes, you do get off days, you do get off days. But take it on the chin and think “Tomorrow, I’m gonna be back up there again.”

Shaun: I’m gonna make a difference.

Carla: Yeah, back up there again. It’s exciting, I just feel excited about life.

Shaun: And I am too.

Carla: Good, brilliant. Thank you, Shaun.

Shaun: Thank you.


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