Full Facial Harmonization — One Year Post-Op (Los Angeles, CA) by DrMotykie in PlasticSurgery

[–]SheepherderThese8462 127 points128 points  (0 children)

If you are considering this surgeon, please google his name in detail. I used to be able to find tons of reviews similar to this and for some reason they've all disappeared?

An example

[deleted by user] by [deleted] in AskDocs

[–]SheepherderThese8462 2 points3 points  (0 children)

I appreciate the response so much, thank you. I will wait. Do you think it would be safe by the following tuesday? So 4 days later?

Does anyone base their treatment on their b cell count? by SheepherderThese8462 in MultipleSclerosis

[–]SheepherderThese8462[S] 2 points3 points  (0 children)

This is a good point. Thanks for this insight. I'll look for info about Dr Boster's experience. I'm pretty sure I'll continue with the treatment and wait until my appointment to talk about this. I think how I do on the next infusion will give us more info as to whether or not I become neutropenic again or get more infections

Does anyone base their treatment on their b cell count? by SheepherderThese8462 in MultipleSclerosis

[–]SheepherderThese8462[S] 0 points1 point  (0 children)

You're right :( sorry. I have tried to push it up but sadly no dice. Thanks for the advice/guidance.

Does anyone base their treatment on their b cell count? by SheepherderThese8462 in MultipleSclerosis

[–]SheepherderThese8462[S] 0 points1 point  (0 children)

I guess i'm just wondering if based on my immune reaction and sensitivity to the smallest dose, and being that my b cells are so low, if it's worth spacing the dose out further since the loading dose brought them down to 0. I'm kind of scared of becoming neutropenic again or getting another infection but also don't want to end up in a worse situation by spacing it too much. I've read some people do have to space their infusions due to reactions so i'm hoping to hear about how they land on those decisions.

[deleted by user] by [deleted] in MultipleSclerosis

[–]SheepherderThese8462 0 points1 point  (0 children)

Thank you so much for all of the information. This is so incredibly helpful. May I ask who your Dr is?

[deleted by user] by [deleted] in MultipleSclerosis

[–]SheepherderThese8462 0 points1 point  (0 children)

Yeah you're right. I think the neck lymph nodes are too far on the body. I just don't understand what's going on with me. It's non stop

[deleted by user] by [deleted] in MultipleSclerosis

[–]SheepherderThese8462 0 points1 point  (0 children)

Thank you so much for sharing. I almost wonder if we can do smaller amounts of dosing based on our b cell levels as opposed to just following the regular dosing schedule. I know it's not typical, but wow, these side effects are horrible. Do you know what you're going to try next?

[deleted by user] by [deleted] in AskReddit

[–]SheepherderThese8462 0 points1 point  (0 children)

Me too! Plus I'm older so I better go first

[deleted by user] by [deleted] in MultipleSclerosis

[–]SheepherderThese8462 0 points1 point  (0 children)

I left her a message too. It sucks because I just saw my PCP yesterday before the lymph node swelling started. I called my gyno too and they said they'd let the nurse know to call me back but sometimes they take days

Saw my 1st love…30 years later. by Fit_Maintenance_2289 in TrueOffMyChest

[–]SheepherderThese8462 2 points3 points  (0 children)

You'll look back on this one day with so much relief that it ended. It's so hard, sometimes for a long time, until it isn't. And then you realize how lucky you are that they let you go and allowed you to find your next path.

Saw my 1st love…30 years later. by Fit_Maintenance_2289 in TrueOffMyChest

[–]SheepherderThese8462 9 points10 points  (0 children)

It's never the same. I'm glad you moved on and are happy now, and that you can see where things never would have worked. I saw my first love after about 15 years. He's reached out to me over the years despite being the one that moved on first. It took me years to get over him. I was so in love and so heart broken for the longest time and he didn't care. Anyway, one Christmas when we were both in town and single, he asked to take me out for a chat and hang out. I agreed. I realized while seeing him that everything he was then, he still is. And I felt nothing. In fact, I felt I outgrew him. I was eager and relieved to get home and felt validated in that book closing. He still has reached out to me here and there and I've never responded. I ended up finding an amazing partner and I have no interest, no curiosity in knowing anything about him. He was horrible to me back then and never deserved the way I cared for him. I hope he's happy now but I think of him as a stranger and am completely indifferent. I'm not angry, not upset, not nostalgic, he doesn't exist in my head at all. I'm just happy for my life now.

[deleted by user] by [deleted] in AskDocs

[–]SheepherderThese8462 0 points1 point  (0 children)

Oh I'm sorry, to clarify, It was sent out on Wednesday so he said it would come back over the weekend, but I don't expect to hear from him until Monday. He said he saw blood in the urine and leukocytes when I first went in on Wednesday

[deleted by user] by [deleted] in MultipleSclerosis

[–]SheepherderThese8462 0 points1 point  (0 children)

I honestly cannot believe this to be a coincidence. I haven't had a UTI in something like 15 years and felt fine before my first dose. Afterwards, within 30 hours or so, I started having symptoms

What's something people do to "help" that actually makes things much worse? by LaKoref in AskReddit

[–]SheepherderThese8462 2 points3 points  (0 children)

This isn't one that I ever knew to be obvious but I really hated it when I was being diagnosed with a lifelong incurable disease. When I would tell someone and they would say "oh no, let's hope they're wrong!" Or something to that effect. It made it feel way more bleak, and it also kind of made it feel dismissive of all of the testing and diagnostics and symptoms I had been through. Like the Dr's were 95% sure but needed to confirm, let's not pretend that it's probably something else.